Stock 129.Cg-Pax6<Sey> Tg(Hbb-b1)83Clo/WsH

FESA Number

1589

Strain Name

129.Cg-Pax6<Sey> Tg(Hbb-b1)83Clo/WsH

Mutation Strain Type

Attribution

Gene/Allele Information

Allele Name Allele MGI ID Gene Name Gene MGI ID Chromosome
Pax6<Sey> MGI:1856155 Pax6 MGI:97490 2
Tg(Hbb-b1)83Clo MGI:2655271 3

Phenotypic Description

Reiterated transgene is detectable by DNA in situ hybridisation.

Publications

Displaying 111 - 120 of 141 Stock Publications
Pubmed ID Authors Title Journal
15548580 Haubst N Molecular dissection of Pax6 function: the specific roles of the paired domain and homeodomain in brain development. Development (2 004) 131:6131-40
10588713 Kioussi C Pax6 is essential for establishing ventral-dorsal cell boundaries in pituitary gland development. Proc Natl Acad Sci U S A (1 999) 96:14378-82
12118260 Muzio L Conversion of cerebral cortex into basal ganglia in Emx2(-/-) Pax6(Sey/Sey) double-mutant mice. Nat Neurosci (2 002) 5:737-45
14762144 Sapir T Pax6 and engrailed 1 regulate two distinct aspects of renshaw cell development. J Neurosci (2 004) 24:1255-64
16289327 Swanson DJ Disruption of cerebellar granule cell development in the Pax6 mutant, Sey mouse. Brain Res Dev Brain Res (2 005) 160:176-93
10498281 Warren N The transcription factor, Pax6, is required for cell proliferation and differentiation in the developing cerebral cortex. Cereb Cortex (1 999) 9:627-35
West JD Transgenic Nomenclature (Correction Mouse Genome 1995;93(1):145) Mouse Genome (1 994) 92:666-668
20016109 Cocas LA Emx1-lineage progenitors differentially contribute to neural diversity in the striatum and amygdala. J Neurosci (2 009) 29:15933-46
11731235 Estivill-Torrús G The transcription factor Pax6 is required for development of the diencephalic dorsal midline secretory radial glia that form the subcommissural organ. Mech Dev (2 001) 109:215-24
25488119 Heavner WE Establishment of the neurogenic boundary of the mouse retina requires cooperation of SOX2 and WNT signaling. Neural Dev (2 014) 9:27

Pages

Orphanet Categories

Rare developmental defect during embryogenesis
Rare urogenital disease
Rare renal disease
Rare eye disease
Rare endocrine disease
Rare oncologic disease
Rare gynecologic or obstetric disease
Rare neurologic disease

EMMA ID

EM:01891

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